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H-2组胺拮抗剂西咪替丁对十二指肠溃疡患者夜间胃酸分泌的抑制作用。一项对照双盲研究。

Inhibition of nocturnal acid secretion in duodenal ulcer patients by an H-2 histamine antagonist-cimetidine. A controlled double-blind investigation.

作者信息

Hollander D, Hossain Z, Sufi A M

出版信息

Am J Dig Dis. 1976 May;21(6):361-5. doi: 10.1007/BF01072656.

Abstract

A new H-2-receptor antagonist, cimetidine, was tested as to its ability to suppress overnight gastric acid secretion in 8 male duodenal ulcer patients. In a double-blind controlled investigation, each volunteer was studied during four consecutive nights. In randomized order they received either 100, 200, or 300 mg of cimetidine or a placebo. No untoward clinical orlaboratory effects of the drug were found. Single-dose oral administration of 300 mg cimetidine caused a significant (P less than 0.05) inhibition of overnight gastric acid secretion for an 8-hr period, with the intragastric pH staying between 3.5-6.0. Cimetidine, because of its potent gastric acid inhibitory effect, may become an important therapeutic agent in the management of peptic ulcer disease.

摘要

一种新型H-2受体拮抗剂西咪替丁,在8名男性十二指肠溃疡患者中进行了抑制夜间胃酸分泌能力的测试。在一项双盲对照研究中,每位志愿者连续四个晚上接受研究。他们按照随机顺序接受100、200或300毫克西咪替丁或安慰剂。未发现该药物有不良临床或实验室效应。单剂量口服300毫克西咪替丁可在8小时内显著(P小于0.05)抑制夜间胃酸分泌,胃内pH值保持在3.5至6.0之间。由于其强大的胃酸抑制作用,西咪替丁可能成为消化性溃疡疾病治疗中的一种重要治疗药物。

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